Patchy particles are patterned particles with at least one well-defined patch that can have highly directional and strongly anisotropic interactions with other particles or surfaces. Multiple theoretical studies point to interesting self-assembly of these particles into superstructures and, as a result, a multitude of possible applications. However, reliable synthetic methods for patchy particles, especially at the sub-micron level, are still a challenge and an active area of research. This work presents a novel synthesis route for making patchy particles at the sub-micron level that involves the use of capillary condensation. Colloidal silica particles of various sizes were synthesized and ordered into closely-packed arrays via evaporative self-assembly. Various chemical agents were capillary condensed into the voids of this assembly which, due to the face-centered cubic structure of the crystallized colloidal silica, produced distinct \patches" on the particle surface. The patches on these particles were successfully functionalized with gold nanoparticles. This method was shown to provide control over the patch size by modifying the silica particle radius, which thermodynamically changes the amount of capillary condensation. The patchy nature of the resultant particles was confirmed using infrared spectroscopy, scanning electron and optical microscopies, energy dispersive x-ray analysis and zeta potential measurements.

Cette thèse de doctorat a pour cadre l'étude des mécanismes physiques qui régissent la propagation d'une fissure dans les verres d'oxydes et questionne notamment l'existence et la portée de mécanismes dissipatifs aux petites échelles. Pour ce faire, la propagation sous critique d'une fissure est pilotée par un chargement en géométrie Double Cleavage Drilled Compression sous environnement contrôlé. Elle fait alors l'objet d'analyses expérimentales in-situ et postmortem sur plus de six décades d'échelles de longueur (du nm au mm) par techniques optiques et microscopie à force atomique (AFM). Une analyse 2D/3D de l'échantillon est réalisée en mécanique linéaire élastique de la rupture pour pouvoir assurer le contrôle à toutes les échelles de l'essai mécanique et exploiter les résultats. L'effet mécanique du condensat capillaire observé par AFM en pointe de fissure est modélisé sur l'exemple du modèle de zone cohésive. Ceci permet d'évaluer la pression de Laplace négative du liquide confiné et d'expliquer le mécanisme de refermeture des fissures. Une technique de corrélation d'image (DIC) est utilisée sur des séries d'images AFM in-situ. Nous montrons que la solution élastique pour le champ de déplacement de surface est valable jusqu'à une distance de 10 nm de la pointe de la fissure. Une étude expérimentale prometteuse de fractoémission a permit l'accès à la taille de la zone d'endommagement nanométrique dans les verres fracturé en régime dynamique. Les fonctions de corrélations de hauteur le long d'images AFM de surfaces de rupture lente ont été analysées. Nous montrons que la longueur de coupure de l'ordre de quelques dizaines de nm, interprétée comme taille de zone d'endommagement, découle plus probablement de la taille finie de la sonde de balayage de l'AFM et qu'en accord avec la DIC, aucune zone d'endommagement de taille supérieure à 20 nm n'est observable. / The aim of this thesis is to study the physical mechanisms which govern crack propagation in oxide glasses and to investigate in particular the existence of dissipative mechanisms at small scales. The subcritical crack propagation is controlled by a loading cell on Double Cleavage Drilled Compression samples under controlled atmosphere. Postmortem and in-situ analysis are performed on more than six decades of length scales (from nm to mm) by optical techniques and atomic force microscopy (AFM). An 2D/3D analysis of this sample is realized according to linear elastic fracture mechanics in order to discuss the experimental results and to ensure the mechanical test control at all scales. The mechanical effect of capillary condensation observed by AFM at the crack tip is modelled according to a cohesive zone model. This allows evaluating the negative Laplace pressure in the liquid and explaining the crack closure mechanism in glass. A digital image correlation technique is used on series of consecutive AFM in-situ images. We show that the elastic solution for the surface displacement field is valid up to a distance of 10 nm from the crack tip. A promising experimental study of fractoemission allowed us to access the nanometric process zone size in glasses during dynamic fracture. The height correlation functions along the AFM images of fracture surfaces were analyzed. We show that the cutoff length, found close to few ten nm and preiously interpreted as the process zone size, is most probably due to the finite size of the AFM scanning probe and in agreement with the DIC, no process zone larger than 20 nm is observable.

No description available.

The aim of this thesis is concerned with the influence of sliding velocity on capillary adhesion at the nanometer scale. In ambient conditions, capillary condensation which is a thermally activated process, allows the formation of a capillary meniscus at the interface between an atomic force microscope (AFM) probe and a substrate. This capillary meniscus leads to a capillary force that acts as an additional normal load on the tip, and affects the adhesion and friction forces. The Atomic Force Microscopy (AFM) offers interesting opportunities for the measurement of surface properties at the nanometer scale. Nevertheless, in the classical imaging mode, limitations are encountered that lead to a non stationary state. These limitations are overcome by implementing a new AFM mode (called Circular AFM mode). By employing the Circular AFM mode, the evolution of the adhesion force vs. the sliding velocity was investigated in ambient conditions on model hydrophilic and hydrophobic surfaces with different physical-chemical surface properties such as hydrophilicity. For hydrophobic surfaces, the adhesion forces or mainly van der Waals forces showed no velocity dependence, whereas, in the case of hydrophilic surfaces, adhesion forces, mainly due to capillary forces follow three regimes. From a threshold value of the sliding velocity, the adhesion forces start decreasing linearly with the logarithm increase of the sliding velocity and vanish at high sliding velocities. This decrease is also observed on a monoasperity contact between a atomically flat mica surface and a smooth probe, thus eliminating the possibility of the kinetics of the capillary condensation being related to a thermally activated nucleation process as usually assumed. Therefore, we propose a model based on a thermally activated growth process of a capillary meniscus, which perfectly explains the experimental results. Based on these results, we focused on directly investigating with the Circular mode the role of capillary adhesion in friction mechanisms. We investigated the influence of the sliding velocity on the friction coefficient, and a decrease following three regimes, similar to the sliding velocity dependence of the capillary adhesion, was observed for hydrophilic surfaces that possess a roughness higher than 0.1 nm. Whereas, an increase of the friction coefficient was observed on hydrophilic (Mica) or hydrophobic (HOPG) atomically flat surfaces that posses a roughness lower than 0.1 nm. However, in this latter case, the three regimes are not established. Finally, on a rough hydrophobic surface, the friction coefficient was sliding velocity independent. A direct comparison with capillary adhesion behavior with the sliding velocity is expected to give new insights to explain this interplay. / The aim of this thesis is concerned with the influence of sliding velocity on capillary adhesion at the nanometer scale. In ambient conditions, capillary condensation which is a thermally activated process, allows the formation of a capillary meniscus at the interface between an atomic force microscope (AFM) probe and a substrate. This capillary meniscus leads to a capillary force that acts as an additional normal load on the tip, and affects the adhesion and friction forces. The Atomic Force Microscopy (AFM) offers interesting opportunities for the measurement of surface properties at the nanometer scale. Nevertheless, in the classical imaging mode, limitations are encountered that lead to a non stationary state. These limitations are overcome by implementing a new AFM mode (called Circular AFM mode). By employing the Circular AFM mode, the evolution of the adhesion force vs. the sliding velocity was investigated in ambient conditions on model hydrophilic and hydrophobic surfaces with different physical-chemical surface properties such as hydrophilicity. For hydrophobic surfaces, the adhesion forces or mainly van der Waals forces showed no velocity dependence, whereas, in the case of hydrophilic surfaces, adhesion forces, mainly due to capillary forces follow three regimes. From a threshold value of the sliding velocity, the adhesion forces start decreasing linearly with the logarithm increase of the sliding velocity and vanish at high sliding velocities. This decrease is also observed on a monoasperity contact between a atomically flat mica surface and a smooth probe, thus eliminating the possibility of the kinetics of the capillary condensation being related to a thermally activated nucleation process as usually assumed. Therefore, we propose a model based on a thermally activated growth process of a capillary meniscus, which perfectly explains the experimental results. Based on these results, we focused on directly investigating with the Circular mode the role of capillary adhesion in friction mechanisms. We investigated the influence of the sliding velocity on the friction coefficient, and a decrease following three regimes, similar to the sliding velocity dependence of the capillary adhesion, was observed for hydrophilic surfaces that possess a roughness higher than 0.1 nm. Whereas, an increase of the friction coefficient was observed on hydrophilic (Mica) or hydrophobic (HOPG) atomically flat surfaces that posses a roughness lower than 0.1 nm. However, in this latter case, the three regimes are not established. Finally, on a rough hydrophobic surface, the friction coefficient was sliding velocity independent. A direct comparison with capillary adhesion behavior with the sliding velocity is expected to give new insights to explain this interplay.

L'objectif de ce travail est de comprendre l'influence des particules très fines sur le phénomène de ré-agglomération lors du broyage. Des billes de verre de taille 0 à 20 µm avec un pourcentage massique variant entre 0 à 1% sont ajoutées dans un tas granulaire de billes de verre de 200 à 300 µm dans un tambour tournant cylindrique de diamètre et longueur 10 cm. La présence des particules fines montre un effet ambivalent sur la stabilité du tas granulaire. Nous avons établi un diagramme de stabilité du milieu granulaire en fonction de la concentration de particules fines et cherché à quantifier l'effet des fines combiné avec d'autres paramètres (humidité relative et vitesse de rotation du tambour). La stabilité d'un tas granulaire dans un tambour tournant est déterminée par la mesure de son angle maximum de stabilité θm. Dans un premier temps, nous avons étudié l'évolution de cet angle à des vitesses de rotation différentes. Les expériences montrent qu'à faible concentration (< 0; 15%), le tas se déstabilise par avalanches lorsque le tambour tourne, θm diminue lorsqu'on augmente la quantité de fines. Quand la vitesse de rotation augmente, le mouvement du tas évolue du régime d'avalanche intermittent au régime d'écoulement continu. En revanche, lorsque la concentration des fines est supérieure à 0,15%, la déstabilisation du tas se traduit par un phénomène de stick-slip à la paroi du tambour, et la quantité de fines augmente la stabilité du tas. Ce comportement apparemment contradictoire est lié au fait que la localisation de la déstabilisation est modifiée. Dans le régime des faibles concentrations, les avalanches commencent à la surface du tas, et le remplissage de l'espace intermédiaire entre les grosses billes par les fines rend la surface de plus en plus lisse, ce qui déstabilise le tas. Par ailleurs, les fines induisent une augmentation de la cohésion du tas par la nucléation des ponts capillaires entre les grains. Ainsi, dans le régime des fortes concentrations, le tas granulaire se comporte comme un corps solide et la déstabilisation a lieu à l'interface tas-tambour. Nous avons également étudié l'influence de l'humidité relative sur la stabilité et montré que dans le régime de faible concentration de particules fines, la déstabilisation est indépendante de l'humidité. D'autre part dans le régime des hautes teneurs en fines, une humidité relative élevée induit une forte cohésion due à la condensation capillaire entre les grains et le tambour ce qui entraîne une augmentation de l'angle maximum de stabilité. / The aim of this work is to understand the effect of very fine particles on the phenomenon of re-agglomeration in the grinding process. Various amount of fine glass beads of 0 to 20 µm (0 to 1% mass concentration) are added to a granular pile of glass beads of 200 to 300 µm rotated in a drum with inner diameter and length of 10 cm. The presence of fine particles shows an ambivalent effect on the stability of the granular heap. We established a stability diagram of the granular medium as a function of fine concentration and quantified the effect of fines combined with other parameters (relative humidity and rotation velocity). The stability of a granular heap in a rotating drum is determined by the measurement of the maximum angle of stability θm. Firstly, we studied the evolution of this angle with different rotation velocities. The experiments indicate that at low fine concentration (< 0:15%), the heap destabilizes through avalanches when the drum rotates, and increasing the fine quantity tends to decrease θm. When the rotation velocity increases, the granular medium transits from intermittent avalanche to continuous flow. In contrast, once the concentration is more than 0:15%, the destabilization of the heap proceeds through a stick-slip phenomenon at the drum wall, and the increase of the fraction of fines tends to increase the stability of the heap. This apparent contradictory behavior is linked to the modification of the destabilization location. In the small concentration regime, the avalanches start at the surface of the heap, and the filling of the interstitial space by the fine particles makes this surface smoother and smoother, thus destabilizing the heap. Besides, the fines induce, through the nucleation of capillary bridges between grains, an increase of the bulk cohesion of the heap. So in the large concentration regime, the heap behaves as a solid body and the destabilization occurs at its bottom. We also studied the influence of relative humidity on the granular stability in our experiment. We found out in the low fine concentration regime, the destabilization is independent of humidity. On the other hand, in the regime of high content of fines, high relative humidity induces a large cohesion due to the capillary condensation between the grains and the wall which induce the increase of the maximum stability angle.

<p></p><p>Biomass and shale gas have been proposed as alternate sources of liquid hydrocarbon fuels. Traditional petroleum refining, however, is not capable of directly converting either the highly oxygenated molecular structure of lignocellulosic biomass or the low molecular weight alkanes of shale gas into liquid fuels. In this work, we investigate two processes to generate fuels by upgrading low molecular weight species present in biomass pyrolysis vapors and in shale gas via carbon-carbon coupling reactions of low molecular weight species present in biomass pyrolysis vapors and shale gas. </p> <p>In the first process, fast pyrolysis and hydrodeoxygenation are used to convert woody biomass into hydrocarbons. However, 22% of the carbon in this process forms C₁-C₃ species which are unsuitable for use as liquid fuels. Aldol condensation has been proposed as a means of leveraging carbonyl groups present in the pyrolysis product distribution prior to hydrodeoxygenation in order to couple low molecular weight species such as glycolaldehyde to transform the C₁-C₃ fraction into C₄₊ species. We demonstrate that aldol condensation of fast pyrolysis vapors results in a large (10%) reduction in carbon yield to C₆ species and only a small (5%) reduction in carbon yield to C₁-C₃ species to form C₇₊ products, suggesting that higher molecular weight species undergo significant reaction over the aldol condensation catalyst. We demonstrate a pathway by which levoglucosan can be converted into levoglucosenone, which then forms C₇₊ species through self-aldol condensation and condensation with light oxygenates. </p> <p>In the second process, light olefins in shale gas, consisting primarily of ethane and propane, are dehydrogenated and oligomerized into higher molecular weight species. Ni cation sites exchanged onto microporous materials catalyze ethene oligomerization to butenes and heavier oligomers, but also undergo rapid deactivation. The use of mesoporous supports has been reported in the literature to alleviate deactivation in regimes of high ethene pressures and low temperatures that cause capillary condensation of ethene within mesoporous voids. Here, we reproduce prior literature findings on mesoporous Ni-MCM-41 and report that, in sharp contrast, reaction conditions that nominally correspond to ethene capillary condensation in microporous Ni-Beta or Ni-FAU zeolites do not mitigate deactivation, likely because confinement within microporous voids restricts the formation of condensed phases of ethene <a>that are effective at solvating and desorbing heavier intermediates that are precursors to deactivation</a>. Deactivation rates are found to transition from a first-order to a second-order dependence on Ni site density in Ni-FAU zeolites with increasing ethene pressure, suggesting a transition in the dominant deactivation mechanism involving a single Ni site to one involving two Ni sites, reminiscent of the effects of increasing H₂ pressure on changing the kinetic order of deactivation in our prior work on Ni-Beta zeolites.</p><br><p></p>

No description available.

Thesis (M. Ing. (Chemical Engineering))--North-West University, Potchefstroom Campus, 2008.

The main objective for the work described in this PhD thesiswas to formulate a friction model to characterize thefrictional behavior of paper. More specifically, the modelshould explain a phenomenon that is typical for paper grades,viz.: that the level of paper-to-paper friction is dependent onthe direction and the number of previous slides. The modelshould also explain the lubricating effect oflow-molecular-mass lipophilic compounds (LLC) that occur inpaper on paper-to-paper friction. Furthermore, the model shoulddescribe the types of forces that influence paper-to-paperfiction and explain the mechanism by which the LLC decreasepaper-to-paper friction. This thesis consists of a literature review of the basicconcepts of tribology and a summary of the main results andconclusions from four studies on the frictional characteristicsof paper and a study on the friction and adhesion of cellulosesurfaces together with some unpublished material. The purpose of the investigation described in the firstpaper was to explain a phenomenon that is typical for papergrades, viz.: the level of paper-to-paper friction is dependenton the direction and the number of previous slides. Thisbehavior is called“friction hysteresis”by theauthors, and it has its origin in the reorientation of thefibers on the surface of a paper and their alignment relativeto the sliding direction. The second paper describes a study that was aimed atidentifying lubricants that occur natively in paper. Filterpapers were impregnated with model compounds representing woodextractives, i.e. low-molecular-weight lipophilic compounds,which are present in wood, pulp and paper, and thepaper-to-paper friction was determined. The results of thatstudy show that a wood extractive must fulfill severalstructural criteria in order to lubricate a paper surface: Itmust have a hydrophilic group that can attach to the papersurface and a linear hydrocarbon backbone of sufficientlength. Although it is not specifically stated in the second paper,the authors proposed a type of lubrication by which woodextractives decrease paper-to-paper friction that is, ineffect, boundary lubrication. The purpose of the investigationdescribed in the third paper was to clarify whether woodextractives and other low-molecular-mass lipophilic compoundsthat occur in paper can act as boundary lubricants on papersurfaces. The main objective of that study was to investigatethe role of chemical structure of LLC for their orientationrelative to the paper surface, which is an important criterionfor boundary lubrication. Filter papers were impregnated withmagnesium salts of different lipophilic acids, which were usedfor model compounds for the LLC. The deposited layers ofmagnesium salts were characterized by X-ray photoelectronspectroscopy (XPS) and contact angle goniometry and thefriction of the impregnated paper sheets was determined. Theresults show that the degree of lubrication and the resistanceto wear of the layers of a magnesium salt increased withincreasing chain length and increasing degree of linearity ofthe lipophilic acid. Based on the results of that study and ofearlier studies, it is concluded that boundary lubrication isthe type of lubrication by which low-molecular-mass lipophiliccompounds that occur natively in paper decreasepaper-to-paper-friction. In boundary lubrication, surfaces are covered withmonolayers of lubricant molecules that comprise an active headgroup that can attach to the surface, e.g. a carboxyl group,and an inert linear backbone, such as a long saturatedhydrocarbon chain. Such compounds form ordered monolayers onsurfaces, so that the backbone points vertically out of planeof the surface. The friction is then determined by theinteractions between the monolayers, which are weaker than theinteractions between the clean surfaces and this gives a lowerfriction. The fourth paper describes a study on the origin of thedifferences in friction levels between different linerboardsbased on recycled fiber (old corrugated container, OCC). Thesheets were subjected to two extraction stages and analyzedwith respect to surface roughness and their content oflow-molecular-mass lipophilic compounds (LLC). The resultsshowed that a high amount of LLC in the sheets lead to lowfriction, due to lubrication. The fifth paper describes a study that was aimed atdetermining the types of forces that influence the frictionbetween the surfaces of hydrophilic polymers and explaining themechanism by which boundary lubricants decrease the friction.The adhesion and the friction of model systems was measuredwith atomic force microscopy (AFM) using regenerated cellulosefilms and functionalised AFM tips and the effect of fatty acidsand humidity was investigated. The friction significantlyincreased with increasing humidity and that there was a strongcorrelation between the ability of a fatty acid to form ahydrophobic surface and its lubricating performance. Measuredadhesion forces at high humidity were well predicted bytheoretical models that took into account the effect of theLaplace pressure acting in a water meniscus formed aroundcontact regions due to capillary condensation. The resultsindicated that the degree of capillary condensation may beeffectively suppressed by increasing the hydrophobicity of thecontacting surfaces, causing adhesion and friction to decrease.These results suggest that friction between paper surfacesunder ambient conditions is greatly influenced by the degree ofcapillary condensation. Furthermore, lubrication by fatty acidsis achieved by the formation of a vertically oriented,hydrophobic monolayer that can withstand the stresses duringsliding and increase the hydrophobicity of the paper surfaceand thereby suppress capillary condensation. <b>Keywords:</b>Friction, paper-to-paper friction, frictionhysteresis, fibers, orientation, sliding direction, woodextractives, low-molecular-mass lipophilic compounds, boundarylubrication, adhesion, capillary condensation, Laplacepressure, surface forces, JKR theory, gas chromatography-massspectroscopy, X-ray photoelectron spectroscopy, contact angle,atomic force microscopy

<p>The main objective for the work described in this PhD thesiswas to formulate a friction model to characterize thefrictional behavior of paper. More specifically, the modelshould explain a phenomenon that is typical for paper grades,viz.: that the level of paper-to-paper friction is dependent onthe direction and the number of previous slides. The modelshould also explain the lubricating effect oflow-molecular-mass lipophilic compounds (LLC) that occur inpaper on paper-to-paper friction. Furthermore, the model shoulddescribe the types of forces that influence paper-to-paperfiction and explain the mechanism by which the LLC decreasepaper-to-paper friction.</p><p>This thesis consists of a literature review of the basicconcepts of tribology and a summary of the main results andconclusions from four studies on the frictional characteristicsof paper and a study on the friction and adhesion of cellulosesurfaces together with some unpublished material.</p><p>The purpose of the investigation described in the firstpaper was to explain a phenomenon that is typical for papergrades, viz.: the level of paper-to-paper friction is dependenton the direction and the number of previous slides. Thisbehavior is called“friction hysteresis”by theauthors, and it has its origin in the reorientation of thefibers on the surface of a paper and their alignment relativeto the sliding direction.</p><p>The second paper describes a study that was aimed atidentifying lubricants that occur natively in paper. Filterpapers were impregnated with model compounds representing woodextractives, i.e. low-molecular-weight lipophilic compounds,which are present in wood, pulp and paper, and thepaper-to-paper friction was determined. The results of thatstudy show that a wood extractive must fulfill severalstructural criteria in order to lubricate a paper surface: Itmust have a hydrophilic group that can attach to the papersurface and a linear hydrocarbon backbone of sufficientlength.</p><p>Although it is not specifically stated in the second paper,the authors proposed a type of lubrication by which woodextractives decrease paper-to-paper friction that is, ineffect, boundary lubrication. The purpose of the investigationdescribed in the third paper was to clarify whether woodextractives and other low-molecular-mass lipophilic compoundsthat occur in paper can act as boundary lubricants on papersurfaces. The main objective of that study was to investigatethe role of chemical structure of LLC for their orientationrelative to the paper surface, which is an important criterionfor boundary lubrication. Filter papers were impregnated withmagnesium salts of different lipophilic acids, which were usedfor model compounds for the LLC. The deposited layers ofmagnesium salts were characterized by X-ray photoelectronspectroscopy (XPS) and contact angle goniometry and thefriction of the impregnated paper sheets was determined. Theresults show that the degree of lubrication and the resistanceto wear of the layers of a magnesium salt increased withincreasing chain length and increasing degree of linearity ofthe lipophilic acid. Based on the results of that study and ofearlier studies, it is concluded that boundary lubrication isthe type of lubrication by which low-molecular-mass lipophiliccompounds that occur natively in paper decreasepaper-to-paper-friction.</p><p>In boundary lubrication, surfaces are covered withmonolayers of lubricant molecules that comprise an active headgroup that can attach to the surface, e.g. a carboxyl group,and an inert linear backbone, such as a long saturatedhydrocarbon chain. Such compounds form ordered monolayers onsurfaces, so that the backbone points vertically out of planeof the surface. The friction is then determined by theinteractions between the monolayers, which are weaker than theinteractions between the clean surfaces and this gives a lowerfriction.</p><p>The fourth paper describes a study on the origin of thedifferences in friction levels between different linerboardsbased on recycled fiber (old corrugated container, OCC). Thesheets were subjected to two extraction stages and analyzedwith respect to surface roughness and their content oflow-molecular-mass lipophilic compounds (LLC). The resultsshowed that a high amount of LLC in the sheets lead to lowfriction, due to lubrication.</p><p>The fifth paper describes a study that was aimed atdetermining the types of forces that influence the frictionbetween the surfaces of hydrophilic polymers and explaining themechanism by which boundary lubricants decrease the friction.The adhesion and the friction of model systems was measuredwith atomic force microscopy (AFM) using regenerated cellulosefilms and functionalised AFM tips and the effect of fatty acidsand humidity was investigated. The friction significantlyincreased with increasing humidity and that there was a strongcorrelation between the ability of a fatty acid to form ahydrophobic surface and its lubricating performance. Measuredadhesion forces at high humidity were well predicted bytheoretical models that took into account the effect of theLaplace pressure acting in a water meniscus formed aroundcontact regions due to capillary condensation. The resultsindicated that the degree of capillary condensation may beeffectively suppressed by increasing the hydrophobicity of thecontacting surfaces, causing adhesion and friction to decrease.These results suggest that friction between paper surfacesunder ambient conditions is greatly influenced by the degree ofcapillary condensation. Furthermore, lubrication by fatty acidsis achieved by the formation of a vertically oriented,hydrophobic monolayer that can withstand the stresses duringsliding and increase the hydrophobicity of the paper surfaceand thereby suppress capillary condensation.</p><p><b>Keywords:</b>Friction, paper-to-paper friction, frictionhysteresis, fibers, orientation, sliding direction, woodextractives, low-molecular-mass lipophilic compounds, boundarylubrication, adhesion, capillary condensation, Laplacepressure, surface forces, JKR theory, gas chromatography-massspectroscopy, X-ray photoelectron spectroscopy, contact angle,atomic force microscopy</p>